Flow cytometry has recently become a choice technique for the quantita
tive analysis of apoptosis. Monoparametric DNA analysis usually allows
identification of apoptotic cells as a ''subdiploid'' peak. Progressi
on through apoptosis leads to chromatin condensation, nuclear fragment
ation and eventually to cell disruption. Thus, a major problem for the
flow cytometric analysis of apoptotic populations is discrimination b
etween debris and apoptotic cells. Here we demonstrate that the best,
parameter on which to make such a distinction is the DNA content, no m
atter what type of cell is studied. In contrast, discrimination betwee
n apoptotic, non-apoptotic cells, and debris is possible on the basis
of scattering signals only in few selected cases, depending on the mor
phology of the intact cells. (C) 1993 Wiley-Liss, Inc.